7klj

Structural highlights

Disease

KI21A_HUMAN Congenital fibrosis of extraocular muscles. The disease is caused by mutations affecting the gene represented in this entry.

Function

KI21A_HUMAN Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity).

See Also

• Kinesin 3D Structures